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NCT06872346Recruiting

Personalized Risk-based Follow-up of Cervical Cancer Screening in Practice, RCT

Personalized Risk-based Follow-up of Cervical Cancer Screening in Practice (PREDICT), Randomized Control Trial

Source: ClinicalTrials.gov · Last updated 7 Aug 2026

Brief summary (registry, in English)

The goal of this PREDICT is to assess a personalize approach to screening and management of cervical cancer testing. The investigators will evaluate patients who are due for a follow up cervical cancer screening in the primary care clinics in the Massachusetts General Brigham system. Patients will be randomized by clinic into three different arms (Arm 1: standard care, Arm 2: visit based reminders, Arm 3: visit based reminders and population health outreach)

Status (registry)
Recruiting
Study type
Interventional
Enrollment
7500 (estimated)
First submitted
28 Feb 2025
Start date
22 Jul 2026
Primary completion date
22 Jul 2028
Lead sponsor
Massachusetts General Hospital
NCT number
NCT06872346

What you commit to

  • Study type: Interventional
  • Planned participants: 7500
  • From 22 Jul 2026 to the primary completion date, 22 Jul 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • were diagnosed with cervical cancer/ CIN3+ prior to the most recent screening Pap or HPV test

Other

  • have had their cervix removed
  • are not English or Spanish-speaking.

Who the study is looking for

  • have a cervix and are 21-70 years old
  • receive care at a participating primary care practice (i.e. PCP team visit within past 3 years)
  • have had a Pap and/ or HPV test within the past 3.5 years
  • has a CCSM result that suggest a 5-year risk of developing CIN3+ that warrants surveillance at 1 or 3 years, diagnostic colposcopy, or treatment (i.e., above average risk).
    • Inclusion of those up to age 70 is intended to identify individuals whose prior history does not meet screening exit criteria, and warrants surveillance or diagnostic care even though women with adequate prior screening can stop at age 65

Age in the registry: 21 years to 70 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Massachusetts General Brigham
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.